Results 31 to 40 of about 25,260 (214)
Nested Selves: Self‐Organization and Shared Markov Blankets in Prenatal Development in Humans
Abstract The immune system is a central component of organismic function in humans. This paper addresses self‐organization of biological systems in relation to—and nested within—other biological systems in pregnancy. Pregnancy constitutes a fundamental state for human embodiment and a key step in the evolution and conservation of our species. While not
Anna Ciaunica +3 more
wiley +1 more source
Copy number variation analysis of twin pairs discordant for cleft lip with or without cleft palate
Non-syndromic cleft lip with or without cleft palate (nsCL/P) is a frequent orofacial malformation. The comparison of concordance rate observed in monozygotic and dizygotic twins supports high level of heritability and a strong genetic component. However,
Luca Scapoli +7 more
doaj +1 more source
Molar incisor hypomineralisation: current knowledge and practice
Background Molar incisor hypomineralisation (MIH) is a common developmental dental condition that presents in childhood. Areas of poorly formed enamel affect one or more first permanent molars and can cause opacities on the anterior teeth. MIH presents a variety of challenges for the dental team as well as functional and social impacts for affected ...
Helen D. Rodd +4 more
wiley +1 more source
Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins
Intestinal atresia in both twins from the same pregnancy is very rare. Only seven pairs of twins have been described. The authors report on two cases of monozygotic twins with different types of intestinal atresia and clinical evolution.
Mario Giuffrè +2 more
doaj +1 more source
Background Although the genomes of monozygotic twins are practically identical, their methylomes may evolve divergently throughout their lifetime as a consequence of factors such as the environment or aging. Particularly for young and healthy monozygotic
Benjamin Planterose Jiménez +6 more
doaj +1 more source
Discordant renal progression of Fabry disease in male monozygotic twins: a case report
Background: Fabry disease (FD) is a rare X-linked lysosomal storage disease caused by mutations in the GLA gene that encodes α-galactosidase A (α-GAL).
Do-Yun Lee +7 more
doaj +1 more source
A Twin Study of Genetic Contributions to Hippocampal Morphology in Schizophrenia
Our goal was to establish whether altered hippocampal morphology represents a trait marker for genetic vulnerability in schizophrenia. We outlined the hippocampi on high-resolution MR images obtained from matched samples of control and discordant ...
Katherine L. Narr +13 more
doaj +1 more source
Indian twin registry: A gold mine for genetic studies
Twins are a source of curiosity, both for the family and the scientific community. Genetic similarities between twins have been the preferred choice to study the heritability of traits.
Ruby Dhar +2 more
doaj +1 more source
Objective: We present a set of twins discordant for low-level mosaic trisomy 17 at amniocentesis, and we review the literature of heterokaryotypic monozygotic twins at amniocentesis.
Chih-Ping Chen +7 more
doaj +1 more source
“Identical” double parathyroid adenomas in monozygotic twins
A number of genes have been associated with sporadic causes of primary hyperparathyroidism. A case of primary hyperparathyroidism secondary to simultaneously presenting double parathyroid adenomas with identical distribution in a set of 48-year-old ...
F. Jeffrey Lorenz
doaj +1 more source

